Variant report

Variant	rs170415
Chromosome Location	chr7:78306561-78306562
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs170416	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs170417	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs321971	0.94[ASN][1000 genomes]
rs321972	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs321974	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs321978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs321980	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs321982	0.96[YRI][hapmap]
rs321989	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs321990	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs321991	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs38101	0.85[JPT][hapmap]
rs38112	0.85[JPT][hapmap]
rs38118	0.85[JPT][hapmap]
rs413001	0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78301800-78307000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:78301800-78321600	Weak transcription	Fetal Brain Female	brain
3	chr7:78304800-78313000	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:78305400-78307200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:78305400-78312400	Weak transcription	Brain Substantia Nigra	brain
6	chr7:78305400-78312800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:78305600-78307000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:78305800-78308200	Weak transcription	Brain Anterior Caudate	brain
9	chr7:78306200-78307400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:78306200-78307400	Enhancers	Osteobl	bone
11	chr7:78306400-78306600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:78306400-78307200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:78306400-78307200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:78306400-78307400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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